MRC/HPA Centre for Environment and Health, Imperial College, UK.
Environ Health. 2009 Nov 30;8:54. doi: 10.1186/1476-069X-8-54.
In spite of decades of epidemiological research, the etiology and causal patterns for many common diseases, such as breast and colon cancer or neurodegenerative diseases, are still largely unknown. Such chronic diseases are likely to have an environmental origin. However, "environmental" risks have been often elusive in epidemiological studies. This is a conundrum for current epidemiological research. On the other side, the relative contribution of genes to chronic diseases, as emerging from GWAS, seems to be modest (15-50% increase in disease risk). What is yet to be explored extensively is a model of disease based on long-term effects of low doses of environmental exposures, incorporating both genetic and acquired susceptibility ("clinical vulnerability"), and the cumulative effects of different exposures. Such a disease model would be compatible with the weak associations found by GWAS and the still elusive role of many (low-level) environmental exposures. We also propose that the introduction of "-omic" high-throughput technologies, such as transcriptomics, proteomics and metabolomics, may provide, in the next years, powerful tools to investigate early effects of environmental exposures and understand the etiology of common diseases better, according to the "clinical vulnerability model". The development of "-omics", in spite of current limitations and lack of sound validation, could greatly contribute to the elucidation of the disease model we propose.
尽管经过了几十年的流行病学研究,但许多常见疾病(如乳腺癌和结肠癌或神经退行性疾病)的病因和因果模式仍在很大程度上不为人知。这些慢性疾病很可能具有环境起源。然而,在流行病学研究中,“环境”风险常常难以捉摸。这是当前流行病学研究的一个难题。另一方面,从 GWAS 中出现的基因对慢性疾病的相对贡献似乎是适度的(疾病风险增加 15-50%)。尚未广泛探索的是一种基于环境暴露低剂量长期影响的疾病模型,该模型结合了遗传和获得性易感性(“临床脆弱性”)以及不同暴露的累积效应。这种疾病模型将与 GWAS 发现的弱关联以及许多(低水平)环境暴露的作用仍然难以捉摸相吻合。我们还提出,引入“组学”高通量技术,如转录组学、蛋白质组学和代谢组学,可能会根据“临床脆弱性模型”,在未来几年为研究环境暴露的早期效应和更好地了解常见疾病的病因提供强大的工具。尽管目前存在局限性和缺乏合理的验证,但“组学”的发展可以极大地促进我们提出的疾病模型的阐明。